United States · FDA National Drug Code directory
Mucinex Nightshift Sinus Maximum Strength
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72854-209_35322ca5-3819-1ec8-e063-6394a90a262f
- Product NDC
- 72854-209
- Form
- TABLET, COATED
- Composition / generic term
- Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride
- Labeler
- RB Health (US) LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250501
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 10 mg/1
- ACETAMINOPHEN — 325 mg/1
- TRIPROLIDINE HYDROCHLORIDE — 1.25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (72854-209-20) / 10 TABLET, COATED in 1 BLISTER PACK · 72854-209-20
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →